A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981533



Internal ID12972278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11265200..11538100hg38UCSC Ensembl
Innerchr9:11265200..11538100hg19UCSC Ensembl
Innerchr9:11255200..11528100hg18UCSC Ensembl
Innerchr9:11255200..11528100hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38272901
hg19272901
hg18272901
hg17272901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752275
Supporting Variants
SamplesBEC_293
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981533
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer